| Literature DB >> 34294847 |
Andrada-Maria Birladeanu1, Malgorzata Rogalska2,3, Myrto Potiri1, Vasiliki Papadaki1, Margarita Andreadou1, Dimitris L Kontoyiannis1,4, Joe D Lewis5, Zoi Erpapazoglou1, Panagiota Kafasla6.
Abstract
In response to oncogenic signals, Alternative Splicing (AS) regulators such as SR and hnRNP proteins show altered expression levels, subnuclear distribution and/or post-translational modification status, but the link between signals and these changes remains unknown. Here, we report that a cytosolic scaffold protein, IQGAP1, performs this task in response to heat-induced signals. We show that in gastric cancer cells, a nuclear pool of IQGAP1 acts as a tethering module for a group of spliceosome components, including hnRNPM, a splicing factor critical for the response of the spliceosome to heat-shock. IQGAP1 controls hnRNPM's sumoylation, subnuclear localisation and the relevant response of the AS machinery to heat-induced stress. Genome-wide analyses reveal that IQGAP1 and hnRNPM co-regulate the AS of a cell cycle-related RNA regulon in gastric cancer cells, thus favouring the accelerated proliferation phenotype of gastric cancer cells. Overall, we reveal a missing link between stress signals and AS regulation.Entities:
Mesh:
Substances:
Year: 2021 PMID: 34294847 DOI: 10.1038/s41388-021-01963-7
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867